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Items: 8

1.

Public perspectives on consent for the linkage of data to evaluate vaccine safety.

Berry JG, Gold MS, Ryan P, Duszynski KM, Braunack-Mayer AJ; Vaccine Assessment Using Linked Data (VALiD) Working Group.

Vaccine. 2012 Jun 13;30(28):4167-74. doi: 10.1016/j.vaccine.2012.04.056. Epub 2012 Apr 27.

PMID:
22546331
2.

Sudden infant death syndrome and unascertainable deaths: trends and disparities among Aboriginal and non-Aboriginal infants born in Western Australia from 1980 to 2001 inclusive.

Freemantle CJ, Read AW, de Klerk NH, McAullay D, Anderson IP, Stanley FJ.

J Paediatr Child Health. 2006 Jul-Aug;42(7-8):445-51.

PMID:
16898883
3.

Patterns, trends, and increasing disparities in mortality for Aboriginal and non-Aboriginal infants born in Western Australia, 1980-2001: population database study.

Freemantle CJ, Read AW, de Klerk NH, McAullay D, Anderson IP, Stanley FJ.

Lancet. 2006 May 27;367(9524):1758-66. Erratum in: Lancet. 2006 Sep 9;368(9539):918.

PMID:
16731271
4.

Interpretation of recent sudden infant death syndrome rates in Western Australia.

Freemantle CJ, Read AW, de Klerk NH, Charles AK, McAullay D, Stanley FJ.

J Paediatr Child Health. 2005 Dec;41(12):669-70.

PMID:
16398872
5.

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.

Callen DF, Eyre HJ, Ringenbergs ML, Freemantle CJ, Woodroffe P, Haan EA.

Am J Hum Genet. 1991 Apr;48(4):769-82. Erratum in: Am J Hum Genet 1991 Aug;49(2):503.

6.

Assignment of the gene for central core disease to chromosome 19.

Haan EA, Freemantle CJ, McCure JA, Friend KL, Mulley JC.

Hum Genet. 1990 Dec;86(2):187-90.

PMID:
2265831
7.

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.

Callen DF, Freemantle CJ, Ringenbergs ML, Baker E, Eyre HJ, Romain D, Haan EA.

Am J Hum Genet. 1990 Sep;47(3):493-8.

8.

Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.

Callen DF, Ringenbergs ML, Fowler JC, Freemantle CJ, Haan EA.

J Med Genet. 1990 Mar;27(3):155-9.

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